Neville John Curtis

Prof. Neville John Curtis

orcid

Research Focus & Metrics

Academic Career Length

50Years (1977-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 1980 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
DCDerrick L. J. Clive
Derrick L. J. Clive
GCGim J. Chittattu
Gim J. Chittattu
VFVittorio Farina
Vittorio Farina
WKWilliam A. Kiel
William A. Kiel
SMSteven M. Menchen
Steven M. Menchen
NCNeville John Curtis
Neville John Curtis

1 September 1980 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
NCNeville John Curtis
Neville John Curtis
RBR. S. Brown
R. S. Brown

15 May 2019 in Minerals
Verified
Journal Article
Open access
PDF file
NCNeville John Curtis
Neville John Curtis
JGJason Gascooke
Jason Gascooke
Martin R. JohnstonMartin R. Johnston
Martin R. Johnston
APAllan Pring
Allan Pring
Our examination of over 230 worldwide opal samples shows that X-ray diffraction (XRD) remains the best primary method for delineation and classification of opal-A, opal-CT and opal-C, though we found that mid-range infra-red spectroscopy provides an acceptable alternative. Raman, infra-red and nuclear magnetic resonance spectroscopy may also provide additional information to assist in classification and provenance. The corpus of results indicated that the opal-CT group covers a range of structural states and will benefit from further multi-technique analysis. At the one end are the opal-CTs that provide a simple XRD pattern (“simple” opal-CT) that includes Ethiopian play-of-colour samples, which are not opal-A. At the other end of the range are those opal-CTs that give a complex XRD pattern (“complex” opal-CT). The majority of opal-CT samples fall at this end of the range, though some show play-of-colour. Raman spectra provide some correlation. Specimens from new opal finds were examined. Those from Ethiopia, Kazakhstan, Madagascar, Peru, Tanzania and Turkey all proved to be opal-CT. Of the three specimens examined from Indonesian localities, one proved to be opal-A, while a second sample and the play-of-colour opal from West Java was a “simple” Opal-CT. Evidence for two transitional types having characteristics of opal-A and opal-CT, and “simple” opal-CT and opal-C are presented.

1 November 1981 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
RBR. S. Brown
R. S. Brown
NCNeville John Curtis
Neville John Curtis
JHJ. Huguet
J. Huguet

1 January 1977 in Journal of the Chemical Society, Chemical Communications
Verified
Journal Article
Closed access
PDF file
DCDerrick L. J. Clive
Derrick L. J. Clive
GCGim Chittattu
Gim Chittattu
NCNeville John Curtis
Neville John Curtis
WKWilliam A. Kiel
William A. Kiel
CWChi Kwong Wong
Chi Kwong Wong
ortho-Alkenyl phenols react rapidly with PhSeCl to produce derivatives of 2,3-dihydrobenzofuran or 3,4-dihydro-2H-benzo[b]pyran (depending on the nature of the ortho-substituent) in a process shown to belong to the general class of cyclofunctionalisations.

1 June 1982 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
RBR. S. Brown
R. S. Brown
DSD. Salmon
D. Salmon
NCNeville John Curtis
Neville John Curtis
SKS. Kusuma
S. Kusuma